FDA 510(k)

OPTHALMIC ENDOSCOPE

K-Number: K832405 · 1983-11-21

Decision Date1983-11-21

Product Code

DecisionSubstantially Equivalent

Device Summary

OPTHALMIC ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1983-11-21 under 510(k) number K832405. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTHALMIC ENDOSCOPE?

OPTHALMIC ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1983-11-21. The listed applicant is Cilco, Inc.. The 510(k) number is K832405.

When did OPTHALMIC ENDOSCOPE receive FDA 510(k) clearance?

OPTHALMIC ENDOSCOPE received FDA 510(k) clearance on 1983-11-21, under 510(k) number K832405.

Who is the listed applicant for OPTHALMIC ENDOSCOPE?

The FDA 510(k) record lists Cilco, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Cilco, Inc. as applicant

K861334CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE K854969CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)K844249K-SOL K843319CILCO I/A SURGICAL PACK K843992CILCOR OPHTHALMIC INSTRUMENTS K843447CILCO DIAMOND KNIFE

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.